Health product recall

Panocell-10, Ficin Treated (2018-01-30)

Starting date:
January 30, 2018
Posting date:
February 9, 2018
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-65944

Affected products

Panocell–10, Ficin Treated

Reason

Immucor has received reports that red blood cells treated with these Ficin solution lots may fail to meet the 3 to 4+ result required when confirming Ficin treatment with the Ficin control. Weak reactions obtained with the control test require repeat of the pre-modification procedure.

Affected products

Panocell-10, Ficin Treated

Lot or serial number
  • 38310-E
  • 40332-E
  • 42355-E
  • 46089-E
  • 48110-E
  • 50135-E
Model or catalog number

0002385

Companies
Manufacturer

Immucor Inc.

3130 Gateway Drive, P.O. Box 5625

Norcross

30091-5625

Georgia

UNITED STATES